Terrasil Itch, Rash and Pain Relief

Product NDC: 24909-163
11-digit product format: 249090163
Labeler code: 24909
Product ID: 24909-163_22ac774a-b61a-4d9b-85f6-3c1e835cdb51
Type: HUMAN OTC DRUG
Nonproprietary name: Allantoin, Lidocaine
Dosage form: KIT
Labeler: Aidance Skincare & Topical Solutions, LLC
Application: part347
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2014-04-18
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	24909-163		I	Inactivated by FDA		2026-10-12
excluded package	package	24909-163	24909-163-25	I	Inactivated by FDA		2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 44 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	24909-163-25	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	24909-163-25	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	24909-163-25	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	24909-163-25	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	24909-163-25	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	24909-163-25	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	24909-163-25	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	24909-163-25	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	24909-163-25	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	24909-163-25	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	24909-163-25	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	24909-163-25	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	24909-163-25	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	24909-163-25	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	24909-163-25	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	24909-163-25	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	24909-163-25	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	24909-163-25	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	24909-163-25	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	24909-163-25	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	24909-163-25	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	24909-163-25	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
24909-163-25	2020-01-31	C162847	48780-1	9d75b9d1-2b35-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
24909-163-25	Terrasil Itch, Rash and Pain Relief	1 in 1 PACKAGE, COMBINATION	KIT	1		1
24909-173-25	Terrasil Itch, Rash and Pain Relief	25 g in 1 TUBE	OINTMENT	25 g	0.5 g in 100g	1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALLANTOIN	ACTIVE INGREDIENT	344S277G0Z	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
LIDOCAINE HYDROCHLORIDE	ACTIVE INGREDIENT	V13007Z41A	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
ALLANTOIN	ACTIVE MOIETY	344S277G0Z	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
LIDOCAINE	ACTIVE MOIETY	98PI200987	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
BENTONITE	INACTIVE INGREDIENT	A3N5ZCN45C	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
COCONUT OIL	INACTIVE INGREDIENT	Q9L0O73W7L	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
ETIDRONATE TETRASODIUM	INACTIVE INGREDIENT	CZZ9T1T1X4	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
JOJOBA OIL	INACTIVE INGREDIENT	724GKU717M	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
LAURIC ACID	INACTIVE INGREDIENT	1160N9NU9U	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
LAVENDER OIL	INACTIVE INGREDIENT	ZBP1YXW0H8	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
MAGNESIUM OXIDE	INACTIVE INGREDIENT	3A3U0GI71G	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
OLIVE OIL	INACTIVE INGREDIENT	6UYK2W1W1E	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
PALM ACID	INACTIVE INGREDIENT	B6G0Y5Z616	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
PALM KERNEL ACID	INACTIVE INGREDIENT	79P21R4317	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
PENTASODIUM PENTETATE	INACTIVE INGREDIENT	961TOZ5L7T	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
PEPPERMINT OIL	INACTIVE INGREDIENT	AV092KU4JH	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SHEA BUTTER	INACTIVE INGREDIENT	K49155WL9Y	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SILVER OXIDE	INACTIVE INGREDIENT	897WUN6G6T	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SODIUM LAURETH SULFATE	INACTIVE INGREDIENT	BPV390UAP0	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SODIUM PALM KERNELATE	INACTIVE INGREDIENT	6H91L1NXTW	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SODIUM PALMATE	INACTIVE INGREDIENT	S0A6004K3Z	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SODIUM STEARATE	INACTIVE INGREDIENT	QU7E2XA9TG	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
WHITE WAX	INACTIVE INGREDIENT	7G1J5DA97F	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
24909-163	TERRASIL ITCH, RASH AND PAIN RELIEF (ALLANTOIN, LIDOCAINE) KIT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]	1	Legacy NDC, 2 package rows	20140501_cef12200-923c-49b2-ab11-ec7d9d0e10d8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1535619	{1 (25000 MG) (allantoin 0.005 MG/MG / lidocaine hydrochloride 0.005 MG/MG Topical Ointment) / 1 (75000 MG) (lidocaine hydrochloride 0.005 MG/MG Medicated Bar Soap) } Pack	GPCK	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535618	allantoin 0.5 % / lidocaine HCl 0.5 % Topical Ointment	PSN	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535619	allantoin 0.5 % / lidocaine HCl 0.5 % Topical Ointment (25 GM) / lidocaine HCl 0.5 % Medicated Bar Soap (75 GM) Pack	PSN	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535617	lidocaine HCl 0.5 % Medicated Bar Soap	PSN	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535618	allantoin 0.005 MG/MG / lidocaine hydrochloride 0.005 MG/MG Topical Ointment	SCD	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535617	lidocaine hydrochloride 0.005 MG/MG Medicated Bar Soap	SCD	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1
1535617	lidocaine HCl 0.5 % Medicated Bar Soap	SY	cef12200-923c-49b2-ab11-ec7d9d0e10d8	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
24909-163-25	24909016325	1 in 1 PACKAGE, COMBINATION		Historical
24909-173-25	24909017325	25 g in 1 TUBE	25 g	Historical